Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g37500 | A01 | 25047161 | C | T | missense_variant | MODERATE | c.592G>A|p.Ala198Thr |
S17 |
2 | BAA01g37500 | A01 | 25047165 | G | A | synonymous_variant | LOW | c.588C>T|p.Leu196Leu |
S15 |
3 | BAA01g37500 | A01 | 25047278 | G | A | synonymous_variant | LOW | c.475C>T|p.Leu159Leu |
S80 |
4 | BAA01g37500 | A01 | 25047292 | C | T | missense_variant | MODERATE | c.461G>A|p.Arg154Lys |
S242 |
5 | BAA01g37500 | A01 | 25048433 | G | A | upstream_gene_variant | MODIFIER | c.-681C>T| |
S13 |
6 | BAA01g37500 | A01 | 25049725 | C | T | upstream_gene_variant | MODIFIER | c.-1973G>A| |
S132 S137 S215 S89 |
7 | BAA01g37500 | A01 | 25051646 | G | A | upstream_gene_variant | MODIFIER | c.-3894C>T| |
S191 |
8 | BAA01g37500 | A01 | 25052033 | G | A | upstream_gene_variant | MODIFIER | c.-4281C>T| |
S189 |
9 | BAA01g37500 | A01 | 25052063 | C | T | upstream_gene_variant | MODIFIER | c.-4311G>A| |
S208 |